Long-term outcomes in patients with advanced melanoma who had initial stable disease with pembrolizumab in KEYNOTE-001 and KEYNOTE-006

被引:22
作者
Hamid, Omid [1 ]
Robert, Caroline [2 ,3 ]
Daud, Adil [4 ]
Carlino, Matteo S. [5 ,6 ,7 ]
Mitchell, Tara C. [8 ]
Hersey, Peter [9 ]
Schachter, Jacob [10 ]
V. Long, Georgina [11 ,12 ,13 ,14 ]
Hodi, F. Stephen [15 ]
Wolchok, Jedd D. [16 ]
Arance, Ana [17 ]
Grob, Jean Jacques [18 ]
Joshua, Anthony M. [19 ,20 ,21 ,22 ]
Weber, Jeffrey S. [23 ]
Mortier, Laurent [24 ]
Jensen, Erin [25 ]
Diede, Scott J. [25 ]
Moreno, Blanca Homet [25 ]
Ribas, Antoni [26 ,27 ]
机构
[1] Angeles Clin & Res Inst, Dept Oncol, 11818 Wilshire Blvd, Los Angeles, CA 90025 USA
[2] Gustave Roussy, Dept Oncol, Serv Dermatol, 114 Rue Edouard Vaillant, F-94805 Villejuif, France
[3] Paris Saclay Univ, 15 Rue Georges Clemenceau, F-91400 Orsay, France
[4] Univ Calif San Francisco, Dept Hematol Oncol, 1600 Divisadero St, San Francisco, CA 94115 USA
[5] Westmead Hosp, Crown Princess Mary Canc Ctr Westmead, 166-174 Hawkesbury Rd, Westmead, NSW 2145, Australia
[6] Blacktown & Mt Druitt Hosp, 166-174 Hawkesbury Rd, Westmead, NSW 2145, Australia
[7] Univ Sydney, Melanoma Inst Australia, Fac Med & Hlth, 40 Rocklands Rd, Sydney, NSW 2065, Australia
[8] Penn Med, Abramson Canc Ctr, Div Hematol & Oncol, 3400 Civ Ctr Blvd,South Pavil,Floor 10, Philadelphia, PA 19104 USA
[9] Univ Sydney, Dept Med, Edward Ford Bldg A27, Sydney, NSW 2006, Australia
[10] Tel HaShomer Hosp, Chaim Sheba Med Ctr Tel HaShomer, Sheba Med Ctr, IL-52621 Ramat Gan, Israel
[11] Univ Sydney, Melanoma Inst Australia, 40 Rocklands Rd, Sydney, NSW 2040, Australia
[12] Univ Sydney, Fac Med & Hlth, Sydney, NSW 2006, Australia
[13] Univ Sydney, Charles Perkins Ctr, Sydney, NSW 2006, Australia
[14] Royal North Shore & Mater Hosp, Pacific Highway, St Leonards, NSW 2065, Australia
[15] Dana Farber Canc Inst, Dept Med Oncol, 450 Brookline Ave, Boston, MA 02215 USA
[16] Mem Sloan Kettering Canc Ctr, Dept Med, 1275 York Ave, New York, NY 10065 USA
[17] Hosp Clin Barcelona, Dept Med Oncol, Carrer Villarroel,170, Barcelona 08036, Spain
[18] Aix Marseille Univ, Hop Timone, Dept Dermatol & Skin Canc, 264 Rue St Pierre, F-13005 Marseille, France
[19] UHN, Princess Margaret Canc Ctr, Dept Med Oncol, 610 Univ Ave, Toronto, ON M5G 2C1, Canada
[20] St Vincents Hosp, Kinghorn Canc Ctr, 370 Victoria St, Darlinghurst, NSW 2010, Australia
[21] UNSW Sydney, St Vincents Clin Sch, 390 Victoria St, Darlinghurst, NSW 2010, Australia
[22] Melanoma Inst Australia, 40 Rocklands Rd, North Sydney, NSW 2065, Australia
[23] NYU Langone Hlth, Laura & Isaac Perlmutter Canc Ctr, 522 1 Ave,Room 1310 Smilow Bldg, New York, NY 10016 USA
[24] Lille Univ, INSERM, U1189, Dept Dermatol, 2 Ave Oscar Lambret, F-59037 Lille, France
[25] Merck & Co Inc, 2000 Galloping Hill Rd, Kenilworth, NJ 07033 USA
[26] Univ Calif Los Angeles, Jonsson Comprehens Canc Ctr, Dept Med, 100 Med Pl Driveway 550, Los Angeles, CA 90095 USA
[27] Univ Calif Los Angeles, David Geffen Sch Med, 100 Med Pl Driveway 550, Los Angeles, CA 90095 USA
关键词
Melanoma; Pembrolizumab; Programmed death 1; PD-1; IPILIMUMAB;
D O I
10.1016/j.ejca.2021.08.013
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: Patients with melanoma and early stable disease (SD) with pembrolizumab have unclear prognosis. We present post hoc analyses of long-term outcomes for patients with early SD, partial response (PR) or complete response (CR) with pembrolizumab. Patients and methods: Patients who received pembrolizumab in the KEYNOTE-001 and KEYNOTE-006 studies and had SD, PR or CR at weeks 12 or 24 were included. Results: Of 294 patients in the week 12 analysis, 107 (36.4%) had SD at week 12, of whom 7 (6.5%) had a best overall response of CR, 43 (40.2%) had PR and 57 (53.3%) had SD. Fortyeight-month overall survival (OS) rates were 95.2%, 73.0% and 47.7%, respectively, for patients with CR, PR and SD at week 12. Similar results were observed in the 241 patients in the week 24 analysis. Forty-eight-month OS rates were 72.1% for patients with SD at week 12 followed by subsequent response and 75.0% for patients with PR at week 12 followed by no change in response or progression. Thirty-six-month and 48-month OS rates were 11.6% and not reached, respectively, for patients with SD at week 12 followed by progression before week 24. Conclusions: A substantial proportion of patients (46.7%) with early (week 12) SD with pembrolizumab achieved subsequent PR or CR. Patients with SD at week 12 and subsequent CR/ PR had similar survival to those who maintained PR. In contrast, patients with SD at week 12 and subsequent progression had poor survival outcomes. These findings may guide treatment decisions for patients achieving early SD. Trial registration: Clinicaltrials.gov: NCT01295827 (KEYNOTE-001); NCT01866319 (KEYNOTE-006). 2021 Merck Sharp & Dohme Corp. and The Author(s). Published by Elsevier Ltd. All rights reserved. This is an open access article under the CC BY-NC-ND license (http:// creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:391 / 402
页数:12
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